ClinVar Miner

List of variants in gene F8 reported as likely benign

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Total variants: 15
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HGVS dbSNP
NM_000132.3(F8):c.*1214G>A rs34700571
NM_000132.3(F8):c.*1416G>T rs186338743
NM_000132.3(F8):c.*29C>T rs5986887
NM_000132.3(F8):c.1086G>A (p.Ala362=) rs1800289
NM_000132.3(F8):c.1508G>A (p.Arg503His) rs35383156
NM_000132.3(F8):c.2214C>T (p.Tyr738=) rs78373805
NM_000132.3(F8):c.2383A>G (p.Arg795Gly) rs2228152
NM_000132.3(F8):c.2535C>A (p.Asp845Glu) rs200316756
NM_000132.3(F8):c.2947G>A (p.Val983Ile) rs35295375
NM_000132.3(F8):c.2994T>G (p.His998Gln) rs149853218
NM_000132.3(F8):c.389-9C>T rs35621875
NM_000132.3(F8):c.4500G>A (p.Pro1500=) rs33921347
NM_000132.3(F8):c.5219+12T>C rs190152270
NM_000132.3(F8):c.6381T>C (p.Asp2127=) rs782214402
NM_000132.3(F8):c.6957G>A (p.Pro2319=) rs200902529

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